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A novel de novo 2.5 Mb microdeletion of 7q22.1 harbours candidate gene for neurobehavioural disorders and mental retardation

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References

  • Al-Hassnan Z. N., Al-Bakheet A., Abu-Dheim N., Al-Younes B., Colak D. and Kaya N. 2011 A novel interstitial microdeletion of 7q22.1-7q22.3 detected by array comparative genomic hybridization. Am. J. Med. Genet. A 155, 3128– 3131.

  • Colella S., Yau C., Taylor J. M., Mirza G., Butler H., Clouston P. et al. 2007 QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data. Nucl. Acids Res. 35, 2013– 2025.

  • De Preter K., Speleman F., Combaret V., Lunec J., Laureys G., Eussen B. H. J. et al. 2002 Quantification of MYCN, DDX1, and NAG gene copy number in neuroblastoma using a real-time quantitative PCR assay. Mod. Pathol. 15, 159–166.

  • Hoebeeck J., van der Luijt R., Poppe B., De Smet E., Yigit N., Claes K. et al. 2005 Rapid detection of VHL exon deletions using real-time quantitative PCR. Lab. Invest. 85, 24–33.

  • Lybaek H., Meza-Zepeda L. A., Kresse S. H., Høysaeter T., Steen V. M. and Houge G. 2008 Array-CGH fine mapping of minor and cryptic HR-CGH detected genomic imbalances in 80 out of 590 patients with abnormal development. Eur. J. Hum. Genet. 16, 1318–1328.

  • Thakker-Varia S. and Alder J. 2009 Neuropeptides in depression: role of VGF. Behav. Brain Res. 197, 262–278.

  • Vermeulen S., Menten B., Van Roy N., Van Limbergen H., De Paepe A., Mortier G. et al. 2004 Molecular cytogenetic analysis of complex chromosomal rearrangements in patients with mental retardation and congenital malformations: delineation of 7q21.11 breakpoints. Am. J. Med. Genet. A. 124, 10–18.

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Correspondence to VAIDAS DIRSE.

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Dirse V., Burnyte B., Gineikiene E., Griskevicius L. and Utkus A. 2014 A novel de novo 2.5 Mb microdeletion of 7q22.1 harbours candidate gene for neurobehavioural disorders and mental retardation. J. Genet. 93, xx–xx

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DIRSE, V., BURNYTE, B., GINEIKIENE, E. et al. A novel de novo 2.5 Mb microdeletion of 7q22.1 harbours candidate gene for neurobehavioural disorders and mental retardation. J Genet 93, 501–503 (2014). https://doi.org/10.1007/s12041-014-0369-9

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  • DOI: https://doi.org/10.1007/s12041-014-0369-9

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